A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576079



Internal ID16363488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77270084..77276431hg38UCSC Ensembl
Innerchr17:75266166..75272513hg19UCSC Ensembl
Innerchr17:72777761..72784108hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg386348
hg196348
hg186348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5786n54
Supporting Variantsnssv876236, nssv876235, nssv876232, nssv876234, nssv876233
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576079
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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